Bladder Cancer Clinical Trial

Using Patient Centered Data and Behavioral Economics to Improve Mobility and Reduce Readmissions After Major Abdominal Surgery

Summary

This is a two-arm randomized, controlled trial during the postoperative period after major abdominal surgery for cancer, including for example radical cystectomy, nephrectomy, colectomy, comparing a control group that uses a wearable device to track physical activity to an intervention group that uses the same wearable devices and receives a supportive social incentive-based gamification intervention to adhere to a step goal program.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Age 18 years or older
diagnosis of cancer undergoing definitive surgical treatment

Exclusion Criteria:

Inability to provide consent
does not have daily access to a smartphone compatible with the wearable device and not willing to use a device that the investigators can provide them
any other medical conditions that would prohibit participation in a physical activity program

Study is for people with:

Bladder Cancer

Estimated Enrollment:

65

Study ID:

NCT04314778

Recruitment Status:

Completed

Sponsor:

University of Pennsylvania

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There is 1 Location for this study

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Abramson Cancer Center
Philadelphia Pennsylvania, 19104, United States
University of Pennsylvania
Philadelphia Pennsylvania, 19104, United States

How clear is this clinincal trial information?

Study is for people with:

Bladder Cancer

Estimated Enrollment:

65

Study ID:

NCT04314778

Recruitment Status:

Completed

Sponsor:


University of Pennsylvania

How clear is this clinincal trial information?

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